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Verfasst von:Pohontsch, Nadine Janis [VerfasserIn]   i
 Schulze, Josefine [VerfasserIn]   i
 Hoeflich, Charlotte [VerfasserIn]   i
 Glassen, Katharina [VerfasserIn]   i
 Breckner, Amanda [VerfasserIn]   i
 Szecsenyi, Joachim [VerfasserIn]   i
 Lühmann, Dagmar [VerfasserIn]   i
 Scherer, Martin [VerfasserIn]   i
Titel:Quality of care for people with multimorbidity
Titelzusatz:a focus group study with patients and their relatives
Verf.angabe:Nadine Janis Pohontsch, Josefine Schulze, Charlotte Hoeflich, Katharina Glassen, Amanda Breckner, Joachim Szecsenyi, Dagmar Lühmann, Martin Scherer
Jahr:2021
Umfang:10 S.
Teil:volume:11
 year:2021
 number:6
 elocationid:e047025
 pages:1-10
 extent:10
Fussnoten:Gesehen am 07.10.2021
Titel Quelle:Enthalten in: BMJ open
Ort Quelle:London : BMJ Publishing Group, 2011
Jahr Quelle:2021
Band/Heft Quelle:11(2021), 6, Artikel-ID e047025, Seite 1-10
ISSN Quelle:2044-6055
Abstract:Background Prevalence of people with multimorbidity rises. Multimorbidity constitutes a challenge to the healthcare system, and treatment of patients with multimorbidity is prone to high-quality variations. Currently, no set of quality indicators (QIs) exists to assess quality of care, let alone incorporating the patient perspective. We therefore aim to identify aspects of quality of care relevant to the patients' perspective and match them to a literature-based set of QIs. Methods We conducted eight focus groups with patients with multimorbidity and three focus groups with patients' relatives using a semistructured guide. Data were analysed using Kuckartz's qualitative content analysis. We derived deductive categories from the literature, added inductive categories (new quality aspects) and translated them into QI. Results We created four new QIs based on the quality aspects relevant to patients/relatives. Two QIs (patient education/self-management, regular updates of medication plans) were consented by an expert panel, while two others were not (periodical check-ups, general practitioner-coordinated care). Half of the literature-based QIs, for example, assessment of biopsychosocial support needs, were supported by participants' accounts, while more technical domains regarding assessment and treatment regimens were not addressed in the focus groups. Conclusion We show that focus groups with patients and relatives adding relevant aspects in QI development should be incorporated by default in QI development processes and constitute a reasonable addition to traditional QI development. Our QI set constitutes a framework for assessing the quality of care in the German healthcare system. It will facilitate implementation of treatment standards and increase the use of existing guidelines, hereby helping to reduce overuse, underuse and misuse of healthcare resources in the treatment of patients with multimorbidity.
DOI:doi:10.1136/bmjopen-2020-047025
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1136/bmjopen-2020-047025
 Volltext: https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=DynamicDOIArticle&SrcApp=WOS&KeyAID=10.1136%2 ...
 DOI: https://doi.org/10.1136/bmjopen-2020-047025
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:centered care
 chronic heart-failure
 disease management programs
 dissemination
 example
 germany
 health-care
 improving primary-care
 indicators
 perceptions
 primary care
 public health
 qualitative research
 quality in healthcare
K10plus-PPN:1772747793
Verknüpfungen:→ Zeitschrift

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